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FDA approves Unloxcyt for advanced skin cancer, first PD-L1 blocker for this use.
The FDA has approved Unloxcyt (cosibelimab-ipdl) by Checkpoint Therapeutics for treating metastatic or locally advanced cutaneous squamous cell carcinoma in patients ineligible for curative surgery or radiation.
It is the first PD-L1 blocking antibody approved for this use.
Common side effects include fatigue, musculoskeletal pain, rash, and diarrhea.
The drug is administered intravenously every three weeks.
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La FDA aprueba Unloxcyt para cáncer de piel avanzado, primer bloqueador de PD-L1 para este uso.